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122,202 results • Page
674 of 2445
Sort: Rank
Rank
Views
Votes
Replies
2
votes
2
replies
2.1k
views
extract UTRs regions from gff file
gff
UTR
updated 4.6 years ago by
heskett
▴ 110 • written 4.6 years ago by
Frieda
▴ 60
1
vote
3
replies
1.5k
views
Differentially expression analysis
rnaseq
DEanalysis
updated 4.6 years ago by
Gordon Smyth
★ 8.6k • written 4.6 years ago by
Sammy
▴ 30
0
votes
0
replies
697
views
Does PRIDE have peptides from nr, RefSeq, or ensembl lnRNAs?
PRIDE
ensembl
peptides
seq
ref
updated 4.6 years ago by
seidel
11k • written 4.6 years ago by
desptsp
• 0
1
vote
2
replies
1.2k
views
Does anyone know how to import 1000 Genomes Project VCF files into usegalaxy.org?
1000genomes
concatenatr
vcf
galaxy
4.6 years ago by
screadore
▴ 20
1
vote
2
replies
1.4k
views
Comparing module topology between two independently constructed networks from wgcna
Comparison
WGCNA
NETWORK
4.6 years ago by
Antonio.Aubry
▴ 10
1
vote
4
replies
1.5k
views
Get the percentage of fragment length that is less than 120bp
CutAndRun
updated 2.7 years ago by
Ram
45k • written 4.6 years ago by
munaj86
▴ 30
0
votes
0
replies
1.3k
views
What are the units for the force output by nstfout, the velocity output by nstvout, and the coordinates output by nstxout in gromacs?
gromacs
md-simulation
4.6 years ago by
honjamaka
• 0
2
votes
3
replies
2.0k
views
Cytoscape: Advice on best analysis methods for PPI network
ontology
network
gene
PPI
cytoscape
updated 4.6 years ago by
qmarulfiz
▴ 60 • written 4.6 years ago by
Haley
▴ 10
0
votes
2
replies
2.3k
views
Plasmid assembly of Oxford nanopore sequencing reads
plasmid
assembly
nanopore
oxford
sequencing
4.6 years ago by
MG_19
• 0
1
vote
1
reply
925
views
Do you know the code for this plot
gene
updated 4.6 years ago by
jared.andrews07
★ 19k • written 4.6 years ago by
zizigolu
★ 4.4k
0
votes
2
replies
791
views
how can I use cytoscape for gene and gene function visualiztion
Cytoscape
RNAseq
GO
4.6 years ago by
BISEP
▴ 10
3
votes
3
replies
1.5k
views
from fasta to gtf format?
gtf
DE
fasta
updated 22 months ago by
e.r.zakiev
▴ 260 • written 4.6 years ago by
debitboro
▴ 270
5
votes
3
replies
1.7k
views
How to calculate the p-value (?) using LRT from codeml output ?
alignment
DNA
Gene
RNA
4.6 years ago by
sunnykevin97
▴ 1000
5
votes
4
replies
2.3k
views
Existing Glycomics/Glycan databases with sugar modifications?
glycomics
database
sugars
updated 4.6 years ago by
ellimilial
▴ 20 • written 7.5 years ago by
Joe
22k
0
votes
6
replies
4.2k
views
What do you do with the data processed after running metaspades/spades?
metaspades
spades
updated 4.6 years ago by
andres.firrincieli
3.9k • written 4.6 years ago by
DNAngel
▴ 260
0
votes
1
reply
1.3k
views
Cannot compile METAL
Meta-analysis
compilation
METAL
updated 4.6 years ago by
GenoMax
154k • written 4.6 years ago by
f-rasmussen
▴ 10
6
votes
7
replies
3.1k
views
Assessing read support for coding sequences predicted by TransDecoder
cds prediction
transdecoder
de novo assembly
updated 4.6 years ago by
ponganta
▴ 590 • written 5.0 years ago by
Dunois
★ 2.9k
4
votes
6
replies
2.1k
views
In need of help with grad school genomic analysis project
project
gradschool
anaylsis
data
updated 4.6 years ago by
qmarulfiz
▴ 60 • written 4.6 years ago by
lopez52891
▴ 10
4
votes
4
replies
1.9k
views
Annotating a genome using a previous annotation file
Annotation
4.6 years ago by
arturo.marin
▴ 20
0
votes
0
replies
757
views
Probabilistic modeling of CpG ß-values
statistics
epigenetics
methylation
updated 4.4 years ago by
Ram
45k • written 4.6 years ago by
lotus28
▴ 70
0
votes
2
replies
1.4k
views
Haplotype Calling Using GATK HaplotypeCaller to Get Exact 35718025 Positions/Loci
GATK
HaplotypeCaller
HaplotypeCalling
4.6 years ago by
yenon118
• 0
0
votes
0
replies
741
views
Measuring diffeences in specific OUTs instead of full smaples in quiime2
OTU
quiime2
4.6 years ago by
blur
▴ 280
0
votes
0
replies
859
views
how to do manual check on retrotransposition insertions with IGV
check
mobile
element
manual
IGV
retrotransposition
4.6 years ago by
jueritation
• 0
0
votes
1
reply
883
views
Technical single-cell question
RNAseq
singlecell
seurat
scRNAseq
updated 4.6 years ago by
ATpoint
90k • written 4.6 years ago by
karen
• 0
0
votes
0
replies
929
views
RFECV (Recursive Feature Elimination with Cross Validation) grid scores discrepancies
RFECV
RFE
CV
4.6 years ago by
ivnnvi
• 0
24
votes
14
replies
21k
views
8 follow
Extracting Subsets Of Reads From A Bam File
bam
samtools
sequencing
updated 3.2 years ago by
Ram
45k • written 13.4 years ago by
ijon.tichy
▴ 80
1
vote
5
replies
2.0k
views
Problem using GenomicRanges package
R
GenomicRanges
updated 2.7 years ago by
Ram
45k • written 4.6 years ago by
tristan.verhoeff
• 0
0
votes
2
replies
1.8k
views
Trimmomatic log file format explanation?
Linux
Trimmomatic
4.6 years ago by
willbrown
• 0
0
votes
0
replies
884
views
Job:
Manager of Laboratory, Safety and Facility Operations
Operations
Safety
Facility
4.6 years ago by
BerkeleyLab
▴ 70
1
vote
3
replies
1.2k
views
problem in creating an object for a list of fasta files
basename
4.6 years ago by
evafinegan
• 0
2
votes
8
replies
2.5k
views
Simple Progress Bar with Alignment
Progress
Hisat2
Alignment
Sequencing
4.6 years ago by
kevin.maroney
• 0
0
votes
1
reply
1.1k
views
GTFtools with Homo_sapiens.GRCh38.103.gtf encoding error in python
GTFtools
Encoding
python3
GRCh38.103
4.6 years ago by
Doreen
• 0
0
votes
0
replies
1.2k
views
Job:
Software Developer
Biophys
Molecular
4.6 years ago by
BerkeleyLab
▴ 70
1
vote
1
reply
2.6k
views
How to analysis 4c seq 3c seq data
3c seq
4c seq
alignment
updated 4.6 years ago by
kalavattam
▴ 380 • written 7.7 years ago by
woongjaej
▴ 30
6
votes
3
replies
1.7k
views
recent Hi-C databases
hi-C
4C
3C
updated 4.6 years ago by
kalavattam
▴ 380 • written 4.9 years ago by
Bogdan
★ 1.4k
2
votes
5
replies
2.8k
views
Bam file metrics
ngs
bam
gatk
updated 4.6 years ago by
Ram
45k • written 4.6 years ago by
Sabeen
▴ 30
4
votes
8
replies
3.3k
views
How to extend ChIP-seq reads from BAM file ?
read-extension
NGS
ChIP-seq
4.6 years ago by
jseg
• 0
0
votes
4
replies
1.8k
views
quick way to get samples that are NOT homozygous reference for a given record using bcftools?
bcftools
4.6 years ago by
curious
▴ 900
8
votes
7
replies
2.6k
views
Whole genome species clustering
phylogeny
assembly
phylogenetics
updated 2.2 years ago by
pmiller
▴ 10 • written 4.6 years ago by
robert.murphy
▴ 110
0
votes
3
replies
1.4k
views
Plink: Number of Samples reducing after merging multiple bed,bim,fam files with Plink's --merge-list function
--merge-list
fam_file
Plink
4.6 years ago by
Swetaleena
• 0
1
vote
2
replies
1.4k
views
single cell RNA QC
scRNA
QC
4.6 years ago by
leranwangcs
▴ 150
0
votes
0
replies
1.3k
views
Need to extract specific VCF sample IDs from 1000Genomes project in the group 30x 1000 genomes genotypes aligned to gr38
1000genomes
extraction
vcf
data
4.6 years ago by
screadore
▴ 20
1
vote
6
replies
2.1k
views
Next Generation Sequencing: in which sequencing technology the read can Not exceed the fragment length?
NGS
Nanopore
Illumina
Pacbio
updated 4.6 years ago by
lieven.sterck
16k • written 4.6 years ago by
FadyNabil
▴ 20
1
vote
1
reply
978
views
How to identify first codon (Methionine) misssense variants?
Mutation
ANNOVAR
Missense
updated 4.6 years ago by
Pierre Lindenbaum
166k • written 4.6 years ago by
lincaijin1994
▴ 50
2
votes
2
replies
1.1k
views
Forum:
What is your experience with the customer support of Oxford University Press?
oup
updated 4.6 years ago by
Kevin Blighe
★ 90k • written 4.6 years ago by
jiri.hon
▴ 20
0
votes
1
reply
1.3k
views
How to solve Warning: [blastx] Taxonomy name
alignment
blastx
warning
blast
updated 4.6 years ago by
GenoMax
154k • written 4.6 years ago by
marongiu.luigi
▴ 770
7
votes
3
replies
3.0k
views
News:
New NCBI Datasets home and documentation pages provide easier access
ncbi
gene
SARS-CoV-2
genome
updated 4.6 years ago by
Istvan Albert
103k • written 4.6 years ago by
e.cox
▴ 50
5
votes
3
replies
2.5k
views
Identification of modules of genes that vary over pseudotime (scRNA-seq pseudotime analysis)
modules
scRNA-seq
singlecell
pseudotime
RNA-seq
updated 4.6 years ago by
jared.andrews07
★ 19k • written 4.6 years ago by
Lucy
▴ 170
1
vote
1
reply
706
views
How align identical sequence from two dataframe in a new dataframe ?
alignment
Rstudio
aminoacid
Identical
sequence
updated 4.6 years ago by
ATpoint
90k • written 4.6 years ago by
Gautier
• 0
0
votes
0
replies
1.1k
views
What is "rl" in SAM format
SAM
format
4.6 years ago by
ymat
• 0
122,202 results • Page
674 of 2445
Recent Votes
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strong appearing variant not found by haplotypecaller in -ERC mode and deepvariant but with haplotypecaller in normal mode
Answer: How can I easily remove overlapping transcripts, keeping only longest transcript
Answer: Log2 transformation is well used, but is there a good paper that can be used as
Answer: Flatten a GTF
Answer: RNA-seq - Creating SAF from NCBI gff for Subread featureCounts - keep 'gene' or
Can EdgeR of DeSeq be used for Single-cell RNA-seq?
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Comment: Visualize methylation status in Pacbio Hifi read
by
cmdcolin
★ 4.4k
(as the JBrowse dev) I'm glad to hear this. if you see any trouble with it feel free to let me know, I have tried to keep up to date with m…
Comment: low quality data or file name swapping -- cellranger arc errors when processing
by
Wu-Sheng Zhang
• 0
Got it! I will try to switch their name and re-run the cellranger arc. Thank you very much, @arup !
Comment: low quality data or file name swapping -- cellranger arc errors when processing
by
Arup Ghosh
3.5k
The barcode files with 24nt read length W71_LUNGrep2_S6_L001_R3_001.fastq.gz and W71_LUNGrep2_S6_L002_R3_001.fastq.gz should be the R2.
Comment: ID unifiying across different datasets
by
GenoMax
154k
Each database has their own method of annotation/validation. Depending on resources available there may be a lag between the databases in t…
Comment: low quality data or file name swapping -- cellranger arc errors when processing
by
Wu-Sheng Zhang
• 0
Hi @arup , thank you very much for your suggestions, and here are the results -- they seems correct. May I have your suggestions? Thank you…
Comment: Why did the QV value decrease significantly after using YAHS for HiC scaffolding
by
samuel.a.odonnell
▴ 640
I don't believe merqury ignores softmasked (lower case) nucleotides so I don't think that is the case. From what it sounds like, during th…
Comment: ID unifiying across different datasets
by
zizigolu
★ 4.4k
Thanks a lot to be helpful I’m trying to build a complete `UniProtID` to `GeneSymbol` lookup table and I’m running into a wall. I’ve alrea…
Comment: strong appearing variant not found by haplotypecaller in -ERC mode and deepvaria
by
thomas.heigl.ibk
▴ 20
thanks for the quick reply. i posted the screenshot. gatk-internally, there is still the difference using -ERC or not, priot is getting …
Comment: strong appearing variant not found by haplotypecaller in -ERC mode and deepvaria
by
thomas.heigl.ibk
▴ 20
here the igv view. showing the histogram for all samples plus the reads for one: ![enter image description here][1] and expanded view of …
Comment: low quality data or file name swapping -- cellranger arc errors when processing
by
Arup Ghosh
3.5k
Check the read lengths to make sure the files are correct.
Comment: strong appearing variant not found by haplotypecaller in -ERC mode and deepvaria
by
Pierre Lindenbaum
166k
> Any suggestions or help you could share please, show us an IGV screenshot of the position GATK realign the reads locally, discards read…
Comment: Can i use orthofinder for small protein datasets and not full proteome?
by
alexandrakortsi
• 0
By sequence. Thank you for your response!
Comment: Why did the QV value decrease significantly after using YAHS for HiC scaffolding
by
xinguok794
▴ 10
Thank you for your reply! Unfortunately, despite running YAHS with `--no-contig-ec`, the QV value of the resulting FASTA file did not impro…
Comment: Subsetting before QC in Spatial Transcriptomics
by
Kent
▴ 30
Hi Kevin, Thanks for the detailed explanation. Due to the characteristics of the datasets, we initially used very lenient quality control…
Comment: Midpoint rooting IQTREE newick file moves node support around
by
Luca Arbore
▴ 10
Thank you very much Kevin, it worked!
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